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Johnson & Johnson, Analyst II, Medical Writing, Immunology - Application via Way
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Johnson & Johnson, Analyst II, Medical Writing, Immunology
Join Johnson & Jhonson to advance innovative medicine as a
Medical Writing Analyst II
in Immunology. This role supports the development of medical documents that communicate clinical findings to regulatory bodies, healthcare professionals and patients. The position offers opportunities to work on early‑ to late‑stage projects, to lead document writing and to contribute to cross‑functional planning and review meetings.
Key Responsibilities
Write and coordinate basic clinical documents including Phase 1 protocols, Phase 1/2 CSRs, tables of studies, narratives and initial Investigator Briefings (IBs).
Contribute to and/or coordinate low to medium complexity clinical and regulatory documents such as Phase 2/3 CSRs, protocols, IB updates, summary documents and regulatory responses under supervision.
Conduct document quality checks, manage abbreviations and references, perform literature searches and support other basic tasks as needed.
Lead written content for early‑ or late‑stage compound writing teams with functional management guidance.
Participate in cross‑functional document planning and review meetings, championing medical‑writing processes and best practices.
Maintain knowledge of applicable industry, company and regulatory guidelines, including ICH requirements and the Medical Writing Style Guide.
Document timelines, project scheduling, and track progress using internal systems.
Attend cross‑functional meetings such as project kick‑offs, study team meetings and Global Program Team meetings.
Complete time reporting, training, and metrics database updates as required.
Qualifications
University or college degree in a scientific discipline (advanced degree such as Master’s, PhD or MD preferred).
Minimum of 2 years of relevant pharmaceutical or scientific experience.
0–4 years of regulatory medical‑writing experience, depending on task complexity and supervision level.
Strong oral and written communication skills with exceptional attention to detail.
Ability to function effectively in a team environment, organize time efficiently, and demonstrate learning agility.
Demonstrated experience summarizing and presenting statistical and medical information with quality and accuracy.
Emerging leadership skills, including project management, time management, influencing and negotiation.
Familiarity with ICH guidance and regulatory submissions.
Compensation & Benefits
Salary range: $89,000 – $143,750 annually.
Eligible for an annual performance bonus per the company’s plan.
Benefits: medical, dental, vision, life insurance, disability coverages, long‑term disability, group legal insurance, 401(k) retirement plan.
Paid time off: up to 120 hours of vacation, 40 hours of sick time per year (56 hours for Washington state residents), 13 days of holiday pay, and floating holidays.
Location
The position is available in multiple locations including the United Kingdom (High Wycombe, Buckinghamshire), Netherlands (Leiden, South Holland), United States (Raritan, New Jersey; Titusville, New Jersey; other U.S. locations as noted). Remote work may be considered on a case‑by‑case basis.
Equal Opportunity
Johnson & Jhonson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other protected status. For accommodations related to disability, please contact us at
https://www.jnj.com/contact-us/careers .
This posting is anticipated to close on September 19, 2025.
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Join Johnson & Jhonson to advance innovative medicine as a
Medical Writing Analyst II
in Immunology. This role supports the development of medical documents that communicate clinical findings to regulatory bodies, healthcare professionals and patients. The position offers opportunities to work on early‑ to late‑stage projects, to lead document writing and to contribute to cross‑functional planning and review meetings.
Key Responsibilities
Write and coordinate basic clinical documents including Phase 1 protocols, Phase 1/2 CSRs, tables of studies, narratives and initial Investigator Briefings (IBs).
Contribute to and/or coordinate low to medium complexity clinical and regulatory documents such as Phase 2/3 CSRs, protocols, IB updates, summary documents and regulatory responses under supervision.
Conduct document quality checks, manage abbreviations and references, perform literature searches and support other basic tasks as needed.
Lead written content for early‑ or late‑stage compound writing teams with functional management guidance.
Participate in cross‑functional document planning and review meetings, championing medical‑writing processes and best practices.
Maintain knowledge of applicable industry, company and regulatory guidelines, including ICH requirements and the Medical Writing Style Guide.
Document timelines, project scheduling, and track progress using internal systems.
Attend cross‑functional meetings such as project kick‑offs, study team meetings and Global Program Team meetings.
Complete time reporting, training, and metrics database updates as required.
Qualifications
University or college degree in a scientific discipline (advanced degree such as Master’s, PhD or MD preferred).
Minimum of 2 years of relevant pharmaceutical or scientific experience.
0–4 years of regulatory medical‑writing experience, depending on task complexity and supervision level.
Strong oral and written communication skills with exceptional attention to detail.
Ability to function effectively in a team environment, organize time efficiently, and demonstrate learning agility.
Demonstrated experience summarizing and presenting statistical and medical information with quality and accuracy.
Emerging leadership skills, including project management, time management, influencing and negotiation.
Familiarity with ICH guidance and regulatory submissions.
Compensation & Benefits
Salary range: $89,000 – $143,750 annually.
Eligible for an annual performance bonus per the company’s plan.
Benefits: medical, dental, vision, life insurance, disability coverages, long‑term disability, group legal insurance, 401(k) retirement plan.
Paid time off: up to 120 hours of vacation, 40 hours of sick time per year (56 hours for Washington state residents), 13 days of holiday pay, and floating holidays.
Location
The position is available in multiple locations including the United Kingdom (High Wycombe, Buckinghamshire), Netherlands (Leiden, South Holland), United States (Raritan, New Jersey; Titusville, New Jersey; other U.S. locations as noted). Remote work may be considered on a case‑by‑case basis.
Equal Opportunity
Johnson & Jhonson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other protected status. For accommodations related to disability, please contact us at
https://www.jnj.com/contact-us/careers .
This posting is anticipated to close on September 19, 2025.
#J-18808-Ljbffr